Clinical Trials Logo
  1. Home
  2. Symptomatic Aortic Stenosis
  3. NCT02803294

Transcatheter Aortic Valve Replacement Single Center Registry in Chinese Population — TORCH  

Symptomatic Aortic Stenosis Clinical Trial

Official title:
THE TORCH TRIAL：Transcatheter Aortic Valve Replacement Single Center Registry in Chinese Population

Clinical Trial Summary

The purpose of this study is to evaluate the safety and effectiveness of transcatheter aortic valve replacement in Chinese population.

Clinical Trial Description

Subjects enrolled are those who undergo physical exams and screening tests and were classified as a patient with symptomatic aortic stenosis or severe aortic regurgitation. They are then performed transcatheter aortic valve replacement. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02803294
Study type Interventional
Source Second Affiliated Hospital, School of Medicine, Zhejiang University
Contact Xianbao Liu, MD
Phone +86-13857173887
Email liuxb2009@hotmail.com
Status Recruiting
Phase Phase 4
Start date June 2016
Completion date July 2027
View Details
See also
  Status Clinical Trial Phase
Completed NCT03003650 - ACURATE TF™ Transfemoral Aortic Bioprosthesis for Implantation in Patients With Severe Aortic Stenosis:CE-approval Cohort N/A
Completed NCT03314857 - China XT: Safety and Effectiveness of Edwards Lifesciences SAPIEN XT THV in the Chinese Population N/A
Active, not recruiting NCT04091048 - Optimize PRO Study
Withdrawn NCT03247465 - Image Fusion and Calcification Raising in Trans Aortic Valve Implantation N/A
Completed NCT03143686 - ACURATE TA™ Valve Implantation: SAVI Registry (Surveillance Plan #2011-02) (TA-SAVI)
Active, not recruiting NCT05182307 - DurAVR™ THV System: First-In-Human Study N/A
Active, not recruiting NCT03466918 - China S3: Safety and Effectiveness of Edwards Lifesciences SAPIEN 3 THV in the Chinese Population N/A
Completed NCT01819181 - Women's INternational Transcatheter Aortic Valve Implantation Registry
Completed NCT04331145 - Platelet REACtivity According to TICagrelor Dose After Transcatheter AorticValve Implantation Phase 4
Completed NCT02536196 - The REFLECT Trial: Cerebral Protection to Reduce Cerebral Embolic Lesions After Transcatheter Aortic Valve Implantation N/A
Recruiting NCT04861805 - Pivotal Study of the Vienna Transcatheter Self Expandable Aortic Valve SE System N/A
Withdrawn NCT02088021 - Assessment of the St. Jude Medical PorticoTM Re-sheathable Aortic Valve System - Alternative Access N/A
Terminated NCT02759237 - The Medtronic Transcatheter Aortic Valve Implant System (CoreValve System Family) Post Marketing Surveillance (PMS) (CoreValve India PMS) N/A
Recruiting NCT01794832 - Severe Aortic Stenosis in Patients Referred for Valve Surgery N/A
Completed NCT02424370 - Geriatric Evaluation to Predict Mortality and Functional Recovery After Trans Aortic Valve Implantation
Completed NCT01493284 - Portico TAVI Implant With Transfemoral Delivery System N/A
Active, not recruiting NCT05712161 - Use of DurAVR™ THV System in Subjects With Severe Aortic Stenosis: Early Feasibility Study N/A
Completed NCT02664649 - Anti-Thrombotic Strategy After Trans-Aortic Valve Implantation for Aortic Stenosis Phase 3
Completed NCT01487330 - First in Human Experience of the St. Jude Medical TAVI Valve and Delivery System N/A
Active, not recruiting NCT04722250 - SMall Annuli Randomized To Evolut™ or SAPIEN™ Trial N/A